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"Philips" electrocardiograph - Taiwan Registration 2901cee77b6f1e2937b682643164a2d3

Access comprehensive regulatory information for "Philips" electrocardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2901cee77b6f1e2937b682643164a2d3 and manufactured by ;; Philips Goldway (Shenzhen) Industrial Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDICAL SYSTEMS, Philips Medizin Systeme Bรถblingen GmbH;; Philips North America LLC, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2901cee77b6f1e2937b682643164a2d3
Registration Details
Taiwan FDA Registration: 2901cee77b6f1e2937b682643164a2d3
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Device Details

"Philips" electrocardiograph
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅฟƒ้›ปๅœ–ๅ„€
Risk Class 2

Registration Details

2901cee77b6f1e2937b682643164a2d3

DHA09200086708

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.2340 Telecardiogram

Input;; Chinese goods

Dates and Status

Aug 25, 2017

Mar 09, 2026